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Journal Abstract Search

135 related items for PubMed ID: 38644274

  • 1. [Efficiency of CNV-seq in detecting fetal DMD gene deletion or duplication in prenatal diagnosis].
    Qiu X, Guo JJ, Jin CC, He J, Wang L, Yang BC, Zhang YH, Zhu BS, Tang XH.
    Zhonghua Fu Chan Ke Za Zhi; 2024 Apr 25; 59(4):279-287. PubMed ID: 38644274
    [Abstract] [Full Text] [Related]

  • 2. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
    Li H, Ding J, Wang W, Chen Y, Lu W, Shao H, Wu BL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun 25; 26(3):318-22. PubMed ID: 19504448
    [Abstract] [Full Text] [Related]

  • 3. [Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy].
    Zhao W, Jiang N, Li S, Li JS, Miao Y, Liang SY, Yu DY.
    Zhonghua Fu Chan Ke Za Zhi; 2019 Apr 25; 54(4):226-231. PubMed ID: 31006187
    [Abstract] [Full Text] [Related]

  • 4. [Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA].
    Zhang Y, Liu X, He R, Ma H, Zhao Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun 25; 31(3):338-43. PubMed ID: 24928015
    [Abstract] [Full Text] [Related]

  • 5. Improved detection of deletions and duplications in the DMD gene using the multiplex ligation-dependent probe amplification (MLPA) method.
    Sansović I, Barišić I, Dumić K.
    Biochem Genet; 2013 Apr 25; 51(3-4):189-201. PubMed ID: 23224783
    [Abstract] [Full Text] [Related]

  • 6. [Clinical value of MLPA in the prenatal gene diagnosis of Duchenne muscular dystrophy].
    Li Q, Li SY, Zhang HM, He WZ, Ma XY, Wang XM, Xian JJ, Sun XF, Chen DJ, Yu YH.
    Zhonghua Fu Chan Ke Za Zhi; 2013 Mar 25; 48(3):161-4. PubMed ID: 23849935
    [Abstract] [Full Text] [Related]

  • 7. Multiplex ligation-dependent probe amplification identification of deletions and duplications of the Duchenne muscular dystrophy gene in Taiwanese subjects.
    Hwa HL, Chang YY, Chen CH, Kao YS, Jong YJ, Chao MC, Ko TM.
    J Formos Med Assoc; 2007 May 25; 106(5):339-46. PubMed ID: 17561468
    [Abstract] [Full Text] [Related]

  • 8. Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA).
    Lai KK, Lo IF, Tong TM, Cheng LY, Lam ST.
    Clin Biochem; 2006 Apr 25; 39(4):367-72. PubMed ID: 16413013
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  • 11. A comparative study of mPCR, MLPA, and muscle biopsy results in a cohort of children with Duchenne muscular dystrophy: a first study.
    Manjunath M, Kiran P, Preethish-Kumar V, Nalini A, Singh RJ, Gayathri N.
    Neurol India; 2015 Apr 25; 63(1):58-62. PubMed ID: 25751470
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  • 12. Multiplex Ligation-Dependent Probe Amplification in X-linked Recessive Muscular Dystrophy in Korean Subjects.
    Suh MR, Lee KA, Kim EY, Jung J, Choi WA, Kang SW.
    Yonsei Med J; 2017 May 25; 58(3):613-618. PubMed ID: 28332368
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  • 13. Molecular Analysis-Based Genetic Characterization of a Cohort of Patients with Duchenne and Becker Muscular Dystrophy in Eastern China.
    Zhao HH, Sun XP, Shi MC, Yi YX, Cheng H, Wang XX, Xu QC, Ma HM, Wu HQ, Jin QW, Niu Q.
    Chin Med J (Engl); 2018 Apr 05; 131(7):770-775. PubMed ID: 29578119
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  • 14. [Mutation screening of 433 families with Duchenne/Becker muscular dystrophy].
    Bai Y, Li S, Zong YN, Li XL, Zhao ZH, Kong XD.
    Zhonghua Yi Xue Za Zhi; 2016 Apr 26; 96(16):1261-9. PubMed ID: 27122458
    [Abstract] [Full Text] [Related]

  • 15. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
    Zhang J, Ma D, Liu G, Wang Y, Liu A, Li L, Luo C, Hu P, Xu Z.
    BMC Med Genet; 2019 Nov 14; 20(1):180. PubMed ID: 31727011
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  • 18. Development of a comprehensive real-time PCR assay for dystrophin gene analysis and prenatal diagnosis of Chinese families.
    Zhang T, Liu S, Wei T, Yong J, Mao Y, Lu X, Xie J, Ke Q, Jin F, Qi M.
    Clin Chim Acta; 2013 Sep 23; 424():33-8. PubMed ID: 23680072
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  • 20. [Unexpected discovery of a fetus with DMD gene deletion using single nucleotide polymorphism array].
    Lin S, Zhou Y, Zhou B, Gu H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug 10; 34(4):563-566. PubMed ID: 28777860
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